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Fruquintinib + tislelizumab is an investigational combination therapy for cancer, particularly being studied in metastatic colorectal cancer and other solid tumors. Fruquintinib is a highly selective, potent oral small-molecule inhibitor of vascular endothelial growth factor receptors 1, 2, and 3 (VEGFR-1/2/3), designed to block tumor angiogenesis and improve tolerability by minimizing off-target effects. Tislelizumab is a humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1), engineered to minimize Fcγ receptor binding on macrophages and reduce T-cell clearance. The combination aims to leverage antiangiogenic effects with immune checkpoint inhibition for synergistic antitumor activity[5][6][8].
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